US5108360A - Monitoring system for medical pump - Google Patents
Monitoring system for medical pump Download PDFInfo
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- US5108360A US5108360A US07/500,150 US50015090A US5108360A US 5108360 A US5108360 A US 5108360A US 50015090 A US50015090 A US 50015090A US 5108360 A US5108360 A US 5108360A
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/50—Details relating to control
- A61M60/585—User interfaces
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/10—Location thereof with respect to the patient's body
- A61M60/122—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body
- A61M60/196—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body replacing the entire heart, e.g. total artificial hearts [TAH]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/40—Details relating to driving
- A61M60/424—Details relating to driving for positive displacement blood pumps
- A61M60/427—Details relating to driving for positive displacement blood pumps the force acting on the blood contacting member being hydraulic or pneumatic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/50—Details relating to control
- A61M60/508—Electronic control means, e.g. for feedback regulation
- A61M60/538—Regulation using real-time blood pump operational parameter data, e.g. motor current
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/50—Details relating to control
- A61M60/508—Electronic control means, e.g. for feedback regulation
- A61M60/538—Regulation using real-time blood pump operational parameter data, e.g. motor current
- A61M60/546—Regulation using real-time blood pump operational parameter data, e.g. motor current of blood flow, e.g. by adapting rotor speed
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/50—Details relating to control
- A61M60/508—Electronic control means, e.g. for feedback regulation
- A61M60/562—Electronic control means, e.g. for feedback regulation for making blood flow pulsatile in blood pumps that do not intrinsically create pulsatile flow
- A61M60/569—Electronic control means, e.g. for feedback regulation for making blood flow pulsatile in blood pumps that do not intrinsically create pulsatile flow synchronous with the native heart beat
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/50—Details relating to control
- A61M60/592—Communication of patient or blood pump data to distant operators for treatment purposes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/80—Constructional details other than related to driving
- A61M60/802—Constructional details other than related to driving of non-positive displacement blood pumps
- A61M60/81—Pump housings
- A61M60/816—Sensors arranged on or in the housing, e.g. ultrasonic flow sensors
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/80—Constructional details other than related to driving
- A61M60/855—Constructional details other than related to driving of implantable pumps or pumping devices
- A61M60/857—Implantable blood tubes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/80—Constructional details other than related to driving
- A61M60/855—Constructional details other than related to driving of implantable pumps or pumping devices
- A61M60/89—Valves
- A61M60/894—Passive valves, i.e. valves actuated by the blood
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2205/00—General characteristics of the apparatus
- A61M2205/33—Controlling, regulating or measuring
- A61M2205/3331—Pressure; Flow
- A61M2205/3334—Measuring or controlling the flow rate
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/10—Location thereof with respect to the patient's body
- A61M60/122—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body
- A61M60/126—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body implantable via, into, inside, in line, branching on, or around a blood vessel
- A61M60/148—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body implantable via, into, inside, in line, branching on, or around a blood vessel in line with a blood vessel using resection or like techniques, e.g. permanent endovascular heart assist devices
Definitions
- the present invention is directed generally to a medical pump for feeding a fluid to a living body and/or pumping or discharging the fluid therefrom and more particularly, though not intended for a limit to this, to an artificial heart, serving as a substitute for a vital heart or as an auxiliary to the vital heart, for circulating blood in vivo.
- an artificial heart Whether the operation of, e.g., an artificial heart is correct or not is of much significance in a medical sense.
- the artificial heart has a rated range of a stroke width in terms of structure. If driven in excess of this range, the artificial heart will undergo serious damages in structure, which probably gives a remarkable hazard to the living body to which the artificial heart is connected.
- the hazardous situation is derived from an excessive expansion of the discharge passage on one hand and an excessive collapse on the other hand.
- the overexpansion causes the discharge to impinge and rub on a casing, with the result that it will be worn away due to a long stretch of use and presumably eventually ruptured.
- an overload is applied on a driving module for driving the artificial heart, and the driving module is thereby damaged electrically or mechanically.
- the overcollapse also presents a high probability that erythrocytes will be destroyed in addition to abrasion caused by rubbing the inner surfaces against each other.
- a system for monitoring operational conditions thereof is required. It is a common practice that an image of a reversible operating body of the artificial heart is displayed on a monitor TV by incorporating a small-sized video camera like a CCD camera into the artificial heart.
- a monitoring system disclosed in Japanese Patent Application No. 62839/1987 is constituted such that movement of the blood is photographed by means of a CCD camera in time series to accumulate the images thereof which are then partly extracted, and these images are arranged in a direction of a time axis to exhibit variations with a passage of time.
- this type of monitoring system also, the correctness or incorrectness of the operation and an availability or unavailability of increase in blood flow rate have to be judged by visually confirming the images. It is therefore difficult to make a judgment from the images formed by photographing the operating body. Besides, a misjudgment tends to be made.
- the operator likewise has to judge an adequateness or inadequateness of the blood flow rate through his visual recognition of the images.
- the judgment from the images of the operating body is effected with difficulty.
- Parts of the artificial heart which are brought into contact with the blood, undergo an antithrombotic treatment to prevent thrombus.
- the blood flows at an adequate velocity under normal using conditions, and there is caused no blood stagnation in contact portions of a blood pump with the blood, thereby producing no thrombus. It is because blood platelets are not activated.
- a flow rate of the blood from the artificial heart is extremely small; or a stroke per heartbeat is small; or an interval between one heartbeat and the next heartbeat is too long even when the stroke suffices, the blood becomes stagnant locally, and a time for which the blood stops in some parts of the discharge passage of the artificial heart.
- a blood pumping flow rate fluctuates.
- a local stagnation of the blood is produced in the suck, where the platelets are activated to cause the thrombus at a high probability.
- stress locally acts on the suck, resulting in a breakage after a long period of time.
- the artificial heart continues to be employed for a relatively long period of time, and hence the above-mentioned system for monitoring the artificial heart is needed.
- the monitoring system is capable of judging an abnormal deformation, an abnormal deflection and a rupture of the suck by visually recognizing time-series configurational variations in the passage image.
- the operator is required to judge the correctness or incorrectness of the suck operation through his visual recognition of the images. It is similarly difficult to make a judgment from the images obtained by photographing the operating body. A misjudgment is likely to be made.
- An arrangement of a monitoring system disclosed in Japanese Patent Laid-Open Publication No. 158864/1985 is that a passage thickness is measured by making use of a Hall element preparatory to conversion into a passage volume, and a flow rate of blood is calculated from variations in the volume which are based on time-series changes in passage thickness.
- a flow rate of the blood ejected by the artificial heart is automatically measured without relying on the judgment by visual observation of the operator, and it follows that the operator does not have to presume the flow rate of the ejected blood.
- the flow rate of the ejected blood depends on conditions of the living body to which the artificial heart is connected as well as on a driving cycle and a driving pressure of the artificial heart. In other words, there are cases where the blood flow rate increases but does not rise particularly when intensifying a drive of the artificial heart. Hence, even if the flow rate of the ejected blood is automatically calculated by measuring the suck thickness in time series, the operator is unable to know whether the flow rate of the ejected blood should be increased or reduced.
- a flow rate of the blood ejected from the artificial heart is automatically measured without relying on the judgment by visual observation of the operator, whereby the operator does not have to presume the flow rate of the ejected blood.
- the properness or unproperness thereof can be determined from the blood flow rate.
- the artificial heart ejects the blood whose amount is greater than a minimum flow rate at which, for example, the platelets are not virtually activated, and if the passage biases on an expanding or contracting side in consequence of its stroke deviating from a normal range, an operating state of the passage varies, and the blood is apt to stagnate partially in the passage.
- Based on the method of measuring the flow rate by means of the monitoring system disclosed in Japanese Patent Laid-Open Publication No. 158864/1985 it is impossible to detect or judge an abnormality in such an operating state.
- the overexpansion or overcollapse of the passage can not automatically be detected. Therefore, the operator has hitherto monitored directly the artificial heart or indirectly through a monitor camera by the visual observation. To be specific, the operator judges the overexpansion or overcollapse in an intellectual manner by visually recognizing a configuration of the pulsating passage. Such a monitoring operation, however, requires a good deal of labor, because the operation has to continue during a period for which the artificial heart works, as a result of which a judgment error or a monitoring mistake is likely to take place.
- a monitoring system for a medical pump having: a reversible operating means for compressing/expanding a space for accommodating a fluid; a discharge port and a suction port which communicate via a non-return valve with the fluid accommodating space; and reversible driving means for driving the reversible operating means, the system comprising: dead center detecting means for detecting at least one of top and bottom dead centers of the reversible operating means; a dead center stopping time measuring means for measuring a time for which the dead center detecting means continue to detect the dead center; and an informing means for informing the time measured by the dead center stopping time measuring means.
- a monitoring system for a medical pump having: a reversible operating means for compressing/expanding a space for accommodating a fluid; a discharge port and a suction port which communicate via a non-return valve with the fluid accommodating space; and reversible driving means for driving the reversible operating means, the system comprising: a stroke detecting means for detecting at least one of discharge and suction strokes of the reversible operating means; a passage detecting means for detecting whether or not a stroke detected by the stroke detecting means traverses predetermined strokes between a set top dead center and a set bottom dead center of the reversible operating means; and an informing means for giving abnormality information in response to a negative result of the detection by the passage detecting means.
- a monitoring system for a medical pump having: a reversible operating means for compressing/expanding a space for accommodating a fluid; a discharge port and a suction port which communicate via a non-return valve with the fluid accommodating space; and reversible driving means for driving the reversible operating means, the system comprising: dead center detecting means for detecting at least one of top and bottom dead centers of the reversible operating means; a passage detecting means for detecting whether or not the dead centers detected by the dead center detecting means exceed set limit points; and an informing means for giving abnormality information in response to an excessive value detected by the passage detecting means.
- a monitoring system for a medical pump having: a reversible operating means for compressing/expanding a space for accommodating a fluid; a discharge port and a suction port which communicate via a non-return valve with the fluid accommodating space; and reversible driving means for driving the reversible operating means, the system comprising: an imaging means for generating image information by photographing the reversible operating means; an image pick-out means for picking out an image of the reversible operating means from the image information generated by the imaging means; a converting means for converting configurational parameters of the image of the reversible operating means which has been picked out by the image pick-out means into a volumetric capacity of a fluid accommodating space defined by the reversible operating means; a variation rate detecting means for detecting a variation rate of the volumetric capacity converted by the converting means; an integrating means for integrating the variation rate detected by the variation rate detecting means; and an informing means for informing
- a monitoring system for a medical pump having: a reversible operating means for compressing/expanding a space for accommodating a fluid; a discharge port and a suction port which communicates via a non-return valve with the fluid accommodating space; and reversible driving means for driving the reversible operating means, the system comprising an imaging means for generating image information by photographing the reversible operating means; an image pick-out means for picking out an image of the reversible operating means from the image information generated by the imaging means; a centroid detecting means for calculating a centroidal position of the image of the reversible means which has been picked out by the image pick-out means; a centroidal deviation detecting means for detecting whether or not the centroidal position calculated by the centroid detecting means fall within a set range; and an informing means for giving corresponding information in response to a negative result of the detection by the centroidal deviation detecting means.
- the following functionsosn are characteristic of a monitoring system for a medical pump according to the present invention. If the top or bottom dead center measured by the dead center stopping time measuring means is long, a flow rate of an ejected fluid is augmented by increasing the nubmer of heartbeats of the artificial heart. The fact that the stopping time is excessively long implies a failure, an abnormality just before the stoppage and a stop abnormality. According to this monitoring system, the informing means informs the operator of a stopping time, whereby the operator is able to judge an availablity or unavailability of increase in the flow rate of the ejected fluid and also the abnormalities in the artificial heart.
- the monitoring system is also arranged such that the stroke detecting means serves to detect the strokes of the reversible operating means, while the passage detecting means detects whether the stroke detected by the stroke detecting means traverses the predetermined stroke. If the detected result is negative, the informing means informs the operator of an abnormality. In both cases (a) and (b), the abnormality information is imparted automatically from the informing means. With this arrangement, there are automatically informed the stroke bias and the local fluid stagnation derived therefrom, which can not automatically be noticed on the basis of the measurement of blood flow rate by the monitoring system disclosed in Japanese Patent Laid-Open Publication No. 58864/1985.
- the reversible oprating means of the medical pump moves with an excessive expansion or contraction, as a result of which the stroke dead centers of the reversible operating means which are detected by the dead center detecting means exceed set limit points.
- the passage detecting means detects this excess, and the informing means issues the abnormality information in response to this detection.
- the operator is able to know the abnormal condition without constantly monitoring the reversible operating means, thereby reducing the labors required for monitoring. Moreover, the probability that an error in judgement and of a monitoring mistake can considerably be decreased.
- a configurational parameter of the image of the reversible operating means which has been formed by the imaging means and picked out by the image pick-out means i.e., a volumetric capacity of the fluid accommodating space defined by the reversible operating means with respect to, for instance, a width or an area exhibits a one-to-one relationship.
- the converting means calculates the volume of the fluid accommodating space.
- the variation rate detecting means detects a variation rate of the volume
- the integrating means integrates the variation rate.
- the integrated values are conceived as a volume variation quantity of the fluid accommodating space sectioned by the reversible operating means for a period from a start of the integration to an end thereof and as an amount of the fluid ejected by the reversible oeprating means.
- a flow rate is given by a fluid quantity/time.
- the informing means informs values proportional to the integrated values. These proportional values are flow rates or values proportional thereto. The flow rates or flow rate corresponding values are informed from the informing means.
- the imaging means is disposed in non-contact with the reversible operating means, and hence there is caused no variation in its operating property and no drop in its durability because of the arrangment that the reversible operating means has no element added. Owing to imaging means and image processing techniques of nowadays, the images of the reversible operating means can accurately be extracted, and a configurational parameter thereof can also exactly be detected. Consequently, the flow rate informed from the informing means becomes precise.
- the centroidal position of an image of the reversible operating means which has been photographed by the imaging mens and picked out by the image pick-out means deviates from the centroidal position at the time of normal operation, viz., from a set range.
- the centroidal deviation detecting means behaves to detect the centroidal deviation, and correspondingly the informing means issues information about the detection.
- the abnormal deformation and deflection appear before the reversible operating means is ruptured, at which time the informing means informs the oeprator of the abnormalities. Therefore, the abnormality notice is issued before the breakage of the reversible operating means.
- the operator visually inspects the medical pump with confirmation in response to the abnormality information. If the pump is abnormal, the medical pump may be replaced. Whereas if normal, the alternative is to adjust a driving pressure of a pump driving module or to check a failure of this driving module or to replace it. The operator is not required to monitor the motions of the medical pump all the time, resulting in reductions both in working burden and in possibility where a judgment error and a monitoring mistake are to be produced.
- FIG. 1 is a block diagram illustrating one embodiment of a monitoring system for a medical pump according to the present invention
- FIGS. 2a to 2c are flowcharts each showing control operations of CPU18 depicted in FIG. 1;
- FIGS. 3a to 3c, 4a, 4b and 5 through 8 are flowcharts each showing control operations of CPU 34 depicted in FIG. 1;
- FIG. 9a is a plan view expessing images of a passage 4 in the form of binary values which are photographed by means of a CCD camera 16;
- FIG. 9b is a plan view illustrating a one-dimensional array A of data representing a stroke Y of a passage 4 which is formed by CPU34, a one-dimensional array B of differential data thereof and a one-dimensional array C of data representing a stopping time T of the passage 4;
- FIG. 9c is a graphic chart depicting a transition Ga of the stroke Y of the passage 4, a transition Gb of a differential value of the stroke Y and a transition of the stroke y when diminishing the stopping time;
- FIGS. 10a through 10d are graphic charts each showing a transition of the stroke Y of the passage 4.
- FIG. 11a is a plan view illustrating an image of the passage 4 and a top dead center value SA used for monitoring a low flow rate abnormality
- FIG. 11b is a plan vie willustrating an image of the passage 4 and a bottom dead center SB used for monitoring the low flow rate adnormality;
- FIG. 11c is a plan view illustrating an image which varies in time series and a contraction cycle allowable maximum value IT;
- FIG. 12a is a vertical sectional view of an artificial heart 1, showing a contraction abnormal state of the passage 4;
- FIG. 12b is a vertical sectional view of the artificial heart 1, showing an expansion abnormal state of the passage 4;
- FIG. 13 is a graphic chart showing a relationship between the stroke Y of the passage 4 and an internal volume Vol of the passage 4;
- FIG. 14a is a plan view depicting a display picture of CRT 53 illustrated in FIG. 1;
- FIGS. 14b and 14c are plan views each partly showing the display picture of CRT 53 of FIG. 1.
- FIG. 1 there is illustrated one embodiment of the monitoring system of the invention.
- a non-return valve which admits an outflow (ejection) of a fluid from the inner space of the passage 4 to the output port 5 but cuts off the fluid flowing in a direction reverse thereto.
- a suction port 6 Interposed between the inner space of the passage 4 and a suction port 6 is a non-return valve which admits an inflow (suction) of the fluid from the suction port 6 to the inner space of the passage 4 but cuts off the fluid flowing in a direction opposte thereto.
- the flexible passage 4 is covered with a transparent internal casing 2.
- an external casing 7 Provided outwardly of the internal casing 2 is an external casing 7 to which light projection ends of optical fibers 8 1 and 8 2 and also a CCD camera 9 are fixed.
- the CCD camera 9 is located on the extension of line of a major axis of the passage 4, a visual field of which is set to accommodate the whole passage 4 including its trail end into a frame.
- the light projection ends of the optical fibers 8 1 and 8 2 are so set that when viewed from the camera 9, an entire outer surface of the passage 4 is illuminated.
- a tube 3 communicating with the inner space of the transparent internal casing 3 is connected to an operating fluid driving pump 13 1 of an artificial hear driving module 10.
- the pump 13 1 alternately imparts a high pressure and a low pressure through an operating fluid (a gas like air in the case of, e.g., Japanese Patent Application No. 85084/1987, or a liquid like silicon oil in the case of, e.g., Japanese Patent Application No. 25371/1989) via the tube 3.
- the operating fluid driving pump 13 1 is electrified by means of a pump driver 12 1 .
- a discharge electrifying duty (discharge period/(discharge period+suction period) ⁇ 100%) at one beat of discharge/suction of the pump driver 12 1 is determined by a pumping controller 11 on the basis of set data given from a data processign computer 33.
- the pumping controller 11 when an asynchronous mode is instructed from the data processing computer 33, drives the pump 13 1 at beats a cycle Tc and a duty (Tp/Tc ⁇ 100% which are specified by the computer 33 in the controller 11. If an outside synchronous mode is instructed, the controller 11 acts to drive the pimp 13 1 at beats synchronizing with synchronous signals (beat pulses of a living body) transmitted from an electrocardiograph or the like.
- the artificial heart driving module 10 are constituted to simultaneously control two pieces of artificial hearts (right and left).
- One artificial heart not illustrated receives high/low pressures given from a pump 13 2 through an operating fluid, while a pump driver 12 2 electrifies the pump 13 2 .
- the CCD camera 9 connected to a camera controller 16 transmits video signals (analog image signals) to the controller 16.
- the controller 16 in turn imparts the video signals to a CRT display 52 and an image processing computer 17. Images of the passage 4 are momentarily displayed on CRT 52.
- the image processing computer 17 behaves to convert the video signals into digital data (gradation data) per frame and write the digital data to a frame memory 24. After writing the data for one frame, the gradation data are binary-coded for conversion into image signals (1 bit for 1 dot: 1 represents black, and 0 represents white). The thus converted image signals are written to A of the frame memory 23.
- the subsequent step is to calculate an address Y1 of an upper fringe of an image of the passage 4 and an address Y2 of a lower fringe thereof in a vertical direction V on the image frame (a picture of the CCD camera). An area S (a portion indicated by oblique lines in FIG. 9a) of the image of the suck 4 is also computed. The thus calculated addresses Y1 and Y2 and the area S are sent to a data processing computer 33.
- FIGS. 3a through 8 there are shown control operations executed by CPUs 34 and 35 of the data processing computer 33.
- FIGS. 2a to 2c illustrates control operations executed by CPUs 18 and 19 of the image processing computer 17.
- CPU 34 of the data processing computer 33 When making a current of a power supply (a step 51: the term “step” will hereinafter be omitted in brackets), CPU 34 sets an I/O port at a signal level when being in a standby state and clears an internal register, a flag register, a timer and a counter 52. CPU 34 then reads a program for executing steps 54 through 86 of a floppy 50 from a floppy disk unit 49 and writes the program to RAM 37 53. The control operation continues to be executed in accordance with a program of RAM 37 till the power supply is turned OFF.
- CRT 53 displays a menu picture an input picture for promoting an operator's input, and inputs of the keyboard 41 are then read 54.
- Inputting is effected in the sequence of the synchronous/asychronouos modes, Tc a beat cycle, Yp a discharge period, SA (a top dead center stroke value for monitoring a low flow rate abnormality in the passage 4: FIG. 11a, SB (a bottom dead center stroke value for monitoring the low flow rate abnormality in the passage 4: FIG. 11b), IT (a contraction cycle allowable maximum value: FIG. 11c), STmax (an expansion peak set value of the passage 4: FIGS. 10a to 10d), STmin (a contraction peak set value of the passage 4: FIGS.
- CPU 34 gives the synchronous/asychronous modes, Tc the beat cycle and Tp the discharge period to the pumping controller 11 of the artificial heart driving module 10, thus giving an instruction of start.
- the artificial heart 1 starts working the passage 4 initiates repetitive contracting and expanding motions alternately at a cycle Tc and a discharge duty given by Tp/Tc ⁇ 100%.
- CPU 34 After starting a drive of the artificial heart 1, CPU 34 issues an image take-in instruction (S1) to the image processing computer 17, which in turn gives an instruction to transfer a binary image signal to DMA 32 of the computer 17 at at timing when the computer 17 writes the binary image signal to A of the memory 23. This is then written to RAM 3 of the memory 42 and is additionally displayed on the menu picture.
- the transmission of the image take-in instruction S1 is repeated at a predetermined cycle, and an instructive indication saying Input the centroidal position of the suck, is added onto the menu picture while updating the display of the passage image.
- a mark (+) is attached to a position specified by the positional data on the display picture of the suck image.
- CPU 34 starts an internal timer to 60 and the clears registers n, k and j for storing data used for judging abnormalities of the passage 4 (A1). Subsequent to this step, CPU 34 starts timers B and D (A2, D1) and permits a receiving interruption for receiving and taking in transmission data Y1, Y2 and S from the computer 17. Then, a subroutine of centroid monitoring 65 is executed. After finishing the execution once, a step of input reading 66 is effected. When an input is given from the keyboard 41, a process corresponding to this input is performed 68. When a stop input is imparted from the keyboard 41, the process is returned to the step 54, where the display on the menu picture resumes. An instruction for stopping is given to the pumping controller 11.
- the process moves back to the step 54, where displaying on the menu picture is effected.
- the operator inputs modification by use of the keyboard 41.
- CPU 34 reads modification at a step of keyboard input reading 66, and the operation moves forward to a subroutine 54, where the menu picture is displayed. The operator adjusts the cursor to a modifying field on the menu picture and inputs modifying information.
- centroid monitoring 65 Provided that no input is given from the keyboard in the subroutine 66, the operation advances to centroid monitoring 65.
- CPU 18 sets an I/O port at a signal level when being in standby state and clears an internal register, a flag register, a timer and a counter (2).
- CPU 18 waits for the image take-in signals S1 coming from the data process computer 33.
- A/D converter 26 converts video signals for one frame which are transmitted from the CCD camera 9 into image data (gradation data) (4), and the thus converted image data are written to the memory 24 (5).
- a binary-coded threshold value of the image data is then set (6).
- the step (6) of setting the binary-coded threshold value begins with creating a histogram, i.e., calculating a sum of densities of image data (density data) per dot with respect to every column in connection with the image data for one frame (256 ⁇ 256 pixels) of the CCD camera.
- a column in which the maximum value of the sum of densities is exhibited is judged, and there is computed a threshold value with which one-fourth of 256 pixels of that column become black (the passage portion).
- the video signals of the CCD camera are read per frame and at the same moment binary-coded to obtain binary-coded data from which an area S (the number of black pixels) of the black region is calculated. A maximum value Sm of the area S is detected.
- the video signals are likewise read per frame and binary-coded for computing the area S.
- a calculated area is equalized virtually to the maximum value Sm, in which case the video signals cease to be read.
- Written to the memory at this time are the image data (gradation data) when the passage 4 expands most (top dead center).
- CPU 18 reduces the threshold value if the area Si is large. Whereas if small, the threshold value is increased.
- the image data of the memory 24 are binary-coded to compute an area Sj thereof.
- the area Sj is then compared with a standard value Ss with the intention of detecting a threshold value with which the area S1 becomes virtually equal to the standard value Ss.
- the thus detected value is set as a threshold value L.
- CPU 18 transmits [Ready] to the data processing computer 33.
- CPU 34 of the data processing computer 33 On receiving [Ready], CPU 34 of the data processing computer 33, as stated earlier, transmits the image take-in signal S2 to the image processing computer 17 at the cycle to.
- CPU 18 of the image processing computer 17 converts the one-frame video signals of the CCD camera 9 into the image data (gradation data) by means of an A/D converter 26 and writes the thus converted image data to the memory 24 (8).
- the image data (one frame) of the memory 24 are binary-coded with a threshold value L preparatory to conversion into binary image signals in which 1 bit (1: black, 0: white) is provided per pixel; and the converted binary image signals are written to A of the memory 23 (9, 10).
- the thus written binary image signals as illustrated in, e.g., FIG. 9a, represent a passage image (oblique lines: black) on the frame picture.
- CPU 18 accesses the binary image signals of the memory 23 column by column from upper and lower ends of the frame toward the center in a horizontal direction (an arrowed direction H).
- the columns in which a ratio of white pixels in one column to black pixels is 1:4 or greater are defined in association with an upper end Y1 and a lower end Y2 respectively (the upper and lower fringes of the passage image) (11 to 33: FIG. 9a).
- the area S (a sum of the black pixels) of the passage image is calculated (34 to 43).
- the upper fringe data Y1, the lower fringe data Y2 and the area data S of the passage image are transferred to the data processing computer 33 (44).
- a flat part of Ga indicates a period for which no variation can be seen in the stroke width.
- a period for which 0 continues in Gb at a one-pulsating cycle is obtained as a stopping time T.
- a mean one-pulsating cycle stopping time Tm for one minute is calculated.
- a maximum value Amax and a minimum value Amin of the strokes are picked out in Ga (FIG. 9c).
- a continuous time (a 0-period in Gb) of the maximum value Amax i.e., a top dead center period Tup
- a continuous time (a 0-period in Gb) of the minimum value Amin viz., a bottom dead center period Tdown (A8).
- One cycle of one beating of the artificial heart 1 is designated at Tc in FIG. 9c, while a period for which the action is effective in discharging the blood is expressed by Tc-(Tup-Tdown).
- Tc-(Tup-Tdown) a period for which the action is effective in discharging the blood
- Tc-(Tup-Tdown) a period for which the action is effective in discharging the blood
- Tc a one pulsating cycle
- Tup and Tdown stopping periods at the top and bottom dead centers respectively
- Tsmall be the smaller of the stopping periods Tu and Tdown.
- An effective acting time Tg for one minute is given by:
- a one pulsating cycle TcD reduced with no variation in the beating quantity is given by:
- a flow rate Fm at which the blood can be pulsed out per minute at the one-pulsating cycle Tc is given such as:
- a flow rate FmD at which the blood can be pulsed out per minute at the one-pulsating cycle TcD is given by:
- a flow rate FI (one minute) increased due to a reduction of the one-pulsating cycle from Tc down to TcD is expressed such as: ##EQU1##
- a heartbeat number Nd per minute for obtaining the one-pulsating cycle TcD is given by:
- FIG. 10a the artificial heart 1 is at full-strokes, and there are dormant periods both in an upper stroke limit and in a lower stroke limit.
- FIGS. 10b through 10d there exists a possibility in which no dormant period of the upper or lower limit is provided, or alternatively no full-stroke is effected both in the upper limit and in the lower limit. Under such circumstances, the flow rate of the artificial heart 1 drops, and in addition, the stroke width is diminished, thereby increasing a possibility of causing the thrombus.
- STmax is the upper limit set value
- STmin is the lower limit set value
- Tup is the upper peak dormant period
- Tdown is the lower peak dormant period.
- CPU 34 functions to calculate the values Tup, Tdown and T in a step A8. Considering these values, among the foregoing cases 0) through 3) CPU 34 judges a case of the driving state of the artificial heart 1.
- the flow rate FI and the heartbeat increasing number NI are calculated (A10 to A18).
- Whether the dormant period T of one-pulsating cycle is more than 5 sec or not is checked (A19). If greater than 5 sec, this implies an operational abnormality.
- a buzzer 51 is energized to display the abnormality caused (the dormant period is excessively long) in a filed (*3) of [ALARM] of a display region DA1 (FIG.
- T, Tup, Tdown, FI and NI are calculated (A3 through A8) after storing the data Y for 150 times in the one-dimensional array A (FIG. 9b and subsequently the data Y for 150 times are stored.
- the mean one-pulsating cycle stopping time Tm is calculated each time the values T, Tup, Tdown, FI and Ni are computed 12 times, and it follows that Tm is updated per minute.
- a predetermined number of the values Tm (for several hours) are held, and trend values thereof are displayed in the display region DA1.
- the buzzer 51 sounds, and simultaneously an alarm message is displayed in the field (*3) of [ALARM] of the display region DA1.
- the buzzer 51 arouses an attention of the operator which in turn can recognize a content of abnormality from the field of [ALARM] of the display region DA1 of CRT 53.
- the duty ratio (Tp/Tc ⁇ 100%: FIG.
- Tp/Tc the duty ratio (Tp/Tc ⁇ 100%: FIG.
- CPU 34 modifies the contents of the display region DA1 to those shown in FIG. 4b, and indicates a message saying [Shortage of an absolute time for feeding out the blood.
- Reduce the heartbeat number N increase Tc) to establish relationships of Tdown>0 and Tup>0, or increase a blood feed-out velocity by rising the driving pressure].
- the absolute time for attaining a full-stroke within one cycle Tc lacks unlike the cases 0) to 2) wherein one cycle Tc includes the dormant period T. It is therefore required to increase the blood feed-out velocity by extending the time Tc of one cycle or augmenting the driving pressure.
- the extension of Tc implies an increase in the heartbeat number N.
- the valve Tup and/or Tdown exceeds 0 by extending Tc or increasing the driving pressure.
- the operating state comes into the cases 0) and 1) or 2) (the operations described above are A22 through A27).
- the heartbeat number N of the artificial heart 1 depends on the number of heartbeats of the living body. Hence, the heartbeat number can not be controlled. Namely, the heartbeat number N (Tc) is unmodifiable in the synchronous mode.
- CPU 34 modifies the contents displayed in the display region DA1 to those shown in FIG. 14c and then indicates a message saying [As the mode is synchronous, the flow rate can not be increased even by changing the driving conditions. The flow rate is kept even by reducing the driving pressure] in a message filed (*2).
- a message of [Shortage of the upper limit stroke When being in the synchronous mode in the case 2), a message of [Shortage of the upper limit stroke.
- a message saying [Shortage of the absolute time for feeding out the blood. Reduce a driving pressure to establish Tdown>0 and Tup>0] is displayed in the message filed (*2) of the display region DA1 depicted in FIG. 14c.
- a variety of the foregoing representations and messages are displayed corresponding to the operating states of the artificial heart 1 by effecting the process of stopping time monitoring (83) described above.
- the operator recognizes the operating state thereof by referring to the display DA1.
- the operator is capable of adjusting the operating state in which to bring about a desired flow rate of the blood to the greatest possible degree by inputting a modifications of the operating condition data through the keyboard 41.
- the blood stagnation is caused in the parts of the artificial heart 1 which contact the blood, thereby easily activating the platelets.
- This facilitates the generating of thrombus; and there is also increased a risk in which the activated platelets are scattered over the respective portions of the living body to clog peripheral blood vessels.
- Detecting the bias of stroke when a normal stroke (e.g., STmax and STmin shown in FIG. 10a) is developed, involves a step of prescribing a set value SA (FIG. 11a) for detecting a stroke abnormality during the expansion and also a set value SB (FIG. 11b) for detecting a stroke abnormality during the contraction.
- SA set value
- SB set value
- the value Sa is smaller than STmax
- SB is greater than STmin, wherein SA>SB.
- the calculated stroke Y undergoes a comparison with the content of the register L each time the stroke Y is newly calculated.
- the stroke Y is updated and written thereto.
- the stroke Y is compared with the content of the register S. If Y is less than the content thereof, the stroke Y is updated and written to the register S (B7).
- Y(Y n+1 ) obtained this time is compared with Y(Yn) computed last time and Y(Y n-1 ) calculated at the before-last time. From these comparative results, there is made a judgment as to whether or not the passage changes from an expanding state to a contracting state, and vice versa (B8, B11).
- a value that is one-half of the content at the time is updated and written to the register L (B10). If a changeover from the contraction to the expansion is performed (at this time the bottom dead center data Amin exists in the register S), whether the data Amin of the register S is less than the value SB or not is checked. If smaller than SB, this implies a normal state. Whereas if more than SB, it is needed that the attention be paid for the thrombus. The buzzer 51 is then energized. A message of [Be cautious about the thrombus.
- Decrease the duty (Tp) (shorten Tp)] is written to RAM 3 of the memory 42 for string the display data of the display region DA63 of CRT 53 and indicated in the [ALARM] field (*4) of the display region DA3 (B12).
- a content of a flag register RC is checked (B13). If the content is 0 (a timer C for measuring time is not yet started), [1] indicating that the timer C is starting is written to a register RC. The timer C is started (B14), and a value that is twice the value thereof at this starting time is written to be register S (B15).
- a time value of the timer C at this time represents a range from the lower peak shown last time to the upper peak indicated this time.
- the time value of the timer C is then compared with IT. If the time value is larger than IT, the buzzer 51 is energized.
- a message saying [Be cautious about the thrombus. Reduction in the pulsating cycle Tc is needed.] is written to RAM 3 of the memory 42 for storing the display data of the display region DA3 of CRT 53 and displayed in the [ALARM] field (a text information display field) (*4) of the display region DA3 (B16).
- the timer C is cleared (B17), and subsequently a register a is cleared (B18).
- the stroke operating mode of the passage 4 is monitored on the basis of the image of the passage 4.
- the buzzer 51 automatically sounds.
- a notice indicating the necessity for paying attention to the thrombus and a countermeasure against it are displayed in the display region DA3 of CRT 53.
- the operator is allowed to modify the driving conditions of the artificial heart 1 via the keyboard 41, referring to these items displayed therein.
- the artificial heart 1 has a rated range of the stroke width Y in terms of structure. If driven in excess of this range, the artificial heart 1 is to undergo structurally serious damages, with the result that the living body will probably be exposed to a remarkably dangerous situation.
- One cause may be an overcollapse, depicted in FIG. 12a, of the passage 4, and the other may be an overexpansion illustrated in FIG. 12b.
- the overcollapse acts to apply excessive stress on the passage 4, which in turn presents a problem pertaining to the mechanical durability thereof and increases the probability that the thrombus occurs due to the easy-to-activate platelets in association with an augment in rubbing action of the suck 4. Whereas in the case of overexpansion, an external surface of the passage 4 impinges and rubs on an inner wall surface of the internal casing 2, resulting in a drop in the mechanical durability of the passage 4.
- the operator inputs the stroke Y calculated in the step 82 in accordance with the subroutine 54 by use of the keyboard 41, while CPU 34 reads this stroke Y and compares it with Smax (an expansion limit value of the passage 4) set in the internal register and Smin (a contraction limit value of the suck 4). If the stroke Y exceeds Smax, an overexpanding abnormality is indicated in the [ALARM] field (*4) of the display region DA3 of CRT 53. When being smaller than Smin, an excessive contraction abnormality is displayed therein. Simultaneously, the buzzer 51 is energized (C4, C6).
- the overexpansion (FIG. 12b) and overcontraction (FIG. 12a) of the passage 4 are automatically detected in the manner described above, thereby informing the abnormalities.
- the operator takes measures, i.e., makes adjustments and inspections of reducing the driving pressure, modifying the duty (changing Tp) and checking the abnormalities in the pump. If a failure can be seen in the artificial heart 1 itself, this artificial heart is replaced with new one. It is feasible to maintain the normal driving state of the artificial heart 1 linked to the living body in this manner and prevent a big accident such as a rupture of the passage 4.
- FIG. 13 shows the data obtained. Referring to FIG. 13, the axis of abscissa indicates a stroke width Y, while the axis of ordinate indicates a volume Vol of the suck 4. In the relationship between the stroke width and the volume in FIG.
- Y can considerably accurately approximately to Vol by a linear or quadratic function.
- CPU 34 updates a content of a count register D up to a value greater by 1 than before (D1).
- Vn associated with the volume Vol of the suck 4 which corresponds thereto is calculated (D2).
- Vf a volume variation quantity obtained by subtracting the volume V n-1 computed last time from the volume Vn computed this time (D3).
- volume variation quantities are written in time series to RAM 2 of the memory 42 and plot-displayed (D4) in a graph display region (*5) of a display region DA2 (FIG. 14a) of CRT 53.
- the plot display exhibits the instantaneous flow rates of the artificial heart 1.
- Vf which represents a discharge flow rate
- Vf represents a suction flow rate
- CPU 34 integrates the flow rates Vf for 2 seconds (60 times) (D5 through D9).
- a suction flow rate per minute is given by multiplying the integrated value by 30. The result is as follows:
- a discharge flow rate per minute is given by:
- the thus calculated values are written to RAM 2 of the memory 42 and displayed in a data display field (*6) of the display region DA2 of CRT 53.
- the integration is effected per 2 sec, and hence the representations of VmI and VmO are updated per 2 sec.
- the discharge flow rate VmO and the suction flow rate VmI of the artificial heart 1 are measured with no addition of a separate measuring instrument such as an electromagnetic flow meter.
- the feeding flow rate is computed on the basis of the stroke Y in the foregoing step of feeding flow rate monitoring (86) but may also be obtained on the basis of the area S of the passage image.
- the one-to-one correspondence is exhibited with respect to the configuration of the passage 4 of the artificial heart 1 and the amount of the blood (an inside volume of the suck 4) with which the passage 4 is filled.
- the area S of an image (drawn with oblique lines in FIG. 9a) of the passage 4 and the blood quantity in the passage 4 similarly show substantially one-to-one correspondence.
- the correspondence of the passage image area to the passage inside volume is experimentally examined to obtain the data in detail.
- centroid monitoring contents of centroid monitoring (65).
- centroid monitoring (65) is executed by the main routine depicted in FIG. 3a.
- the step of centroid monitoring (65) requires a relatively good deal of arithmetic time for computing the centroids, and therefore the execution is performed by the main routine so as not to give a virtual restraint to an executing time for one process.
- the image data are then binary-coded to obtain binary image signals for one frame which are to be written to RAM A of a frame memory 23. Therefore, the binary image signals for one frame of RAM A of the frame memory 23 are updated at a cycle to.
- centroid calculation of the passage image shown by the binary image signals for one frame Assuming that one process (a centroid calculation of the passage image shown by the binary image signals for one frame) of centroid monitoring (65) is not finished within to, a target picture for calculating the centroid is varied in this case, resulting in an error of the centroid calculation.
- the binary image signals for one frame are written to RAM B of the frame memory 23 so that the target picture is not changed during one process. Based on the thus written binary image signals, the arithmetic operation of the centroid is effected.
- CPU 34 at first gives DMA 32 of the image processing computer 17 an instruction to write the data of RAM A of the memory 23 to RAM B. Upon a completion of writing, CPU 34 issues an instruction to transfer the data of RAM A, which data are then written to RAM 2 (particularly to a memory region directed to a pixel display region *7 of the display region DA3 thereof). Image data marked with (+), to which blue display information is added, are additionally written in a specified centroidal position (a, b) which has previously been inputted and held in the step of reading an input by the operator and setting the data (54) and then displayed in the display region DA3 (particularly in the pixel display region *7 thereof) of CRT 53 (F1).
- CPU 34 causes an arithmetic CPU 35 to compute a moment M (1, 0), with respect to I-axis, of a two-dimensional distribution of a group of black pixels of the binary image signals of RAM B of the memory 42 on the assumption that a single piece of black pixel has a weight of 1 (F2). Similarly, CPU 35 computes a moment M (0, 1) with respect to a J-axis (F3) and an area M (0, 0) (F4). CPU 34 further causes CPU 35 to calculate a present position (m, n) of the centroid (F5). Note that in these arithmetic and calculating operations, CPU 34 instructs DMA 32 to transfer, to CPU 35, the binary image signals of necessary parts on the suck image picture (information of RAM B of the memory 23).
- CPU 34 when acquiring the present centroidal position (m, n), additionally writes the (+) marked image data to which red display information is added in the present position (m, n) of the pixel display region *7 of the display region DA3 of RAM 3 of the memory 42, the image data being displayed in the display region DA3 (particularly in the pixel display region *7 thereof) of CRT 53) (F1).
- CPU 34 checks whether or not the present centroidal position (m, n), i.e., the red (+) mark is within +5 (pixel) both in a horizontal direction (H) and in a vertical direction (V) of the input centroidal position, viz., the blue (+) mark (F6). If deviated from that range, the buzzer 51 is energized, and a message (text information) of [passage abnormality. Inspect the artificial heart immediately.] is written to RAM 3 of the memory 42. This message is then displayed in an [ALARM] field (a text information display field) *4 of the display region DA3 of CRT 53 (F7).
- AARM a text information display field
- the step of centroid monitoring (65) described above is repeatedly executed when internal timer interruption (70) and receiving interruption (80) are not yet executed by the main routine (FIG. 3a). Each time the repetition is carried out, there are updated the items, i.e., the passage image, the specified centroidal position (blue (+) mark) and the present centroidal position (red (+) mark) which are indicated in the pixel image display region *7 of the display region DA3 of CRT 53. If the present centroidal position (red (+) mark) deviates from a range of +5 pixels in the vertical direction (V) and in the horizontal direction (H) about the specified centroidal position (blue (+) mark), the buzzer 51 begins sounding, and a piece of text information saying [passage abnormality. Inspect the artificial heart immediately.] is displayed in the [ALARM] display field *4 of the display region DA3 of CRT 53.
- a configuration and a thickness of the artificial heart 1 show a point symmetry virtually with respect to the centroidal position during the operation thereof. Since the passage 4 itself has a self-restoring property of configuration, the centroidal position of the passage 4 is kept substantially constant when the passage 4 is driven within a rated range under a non-failure condition. Hence, if a large centroidal deviation takes place, there may be created such situations that the internal casing 2 comes off or is broken or deformed; or the passage 4 itself is deformed or broken; or the artificial heart driving module 10 is abnormally driven due to a deviation from a rated range or undergoes a failure. In any case, those conditions probably lead to accidents.
- the attention of the operator is aroused by a sound of the buzzer 51, and therefore the operator visually confirms a content of abnormality and a positional deviation or deformation of the passage 4.
- the operator immediately investigates a cause for the abnormality and can take a quick measure.
- the multiple information indicating the operating states of the artificial heart 1 and the information on countermeasures are displayed on the display surface of CRT 53.
- the items in the display region DA1 will be changed to those shown in FIGS. 14b and 14c as the case may be.
- Shown in a display region DA4 is a graphic display of 150 pieces of stroke Y data (one-dimensional array A) in time series (of samplings at a cycle to) of Y in a step A6 of stopping time monitoring (83) in connection with CPU 34.
- This graphic display corresponds to a graph depicted in the uppermost field of FIG. 9c.
- RAM 1 is set to store contents which are to be displayed in the display region DA1;
- RAM 2 stores those stored in the display region DA2;
- RAM 3 stores those displayed in the display region DA3;
- RAM 4 stores those displayed in the display region DA4.
- Display forms (frame lines, display titles, items, etc.) are fixed.
- the information for displaying the forms is originally written to a floppy 50 and read to the data processing computer 33.
- the information is further written to RAM 45.
- the forms displayed in the display region DA1 are read from RAM 45 and written to RAM 1 of the memory 42 in conformity with judgments about the asynchronous/synchronous modes in stopping time monitoring (83) and judgments in the cases 0) through 3).
- the display forms of the display regions DA2 to DA4 are, since they are fixed, written to RAMs 2 through 4 of the memory 42 when being written to RAM 45.
- the monitoring system includes; the dead center detecting means (9, 17 and 33) for detecting at least one of the top and bottom dead centers of the reversible operating means (4) of the medical pump (1); the dead center stopping time measuring means (33) for measuring a time for which the dead center detecting means (9, 17 and 33) continue to detect the dead centers; and the informing means (53) for informing the time measured by the dead center stopping time measuring means (33).
- the dead center stopping time measuring means (33) measures a stopping time of the top and/or bottom dead center, and the informing means (53) in turn informs this time value.
- the operator is capable of judging the availability or unavailability of an increase in the flow rate of the fluid fed out and abnormalities of the artificial heart.
- the operator is able to recognize the availability or unavailability of the increase in the flow rate and the abnormalities without constant visual observation of the operating state of the artificial heart and presumptively grasping a situation on the basis of this visual observation, thereby reducing both troubles derived from a mistake of judgment by the operator and working burdens on the operator.
- the stroke detecting means (34) detects the strokes of the reversible operating means (4), while the passage detecting means (34) detects whether or not the strokes (Amax, Amin) detected by the stroke detecting means (34) traverse the predetermined strokes (SA, SB). If a result of the detection is negative, the informing means (53) gives the abnormality information.
- the informing means (3) automatically imparts the information indicating the abnormalities in such cases that the stagnation tends to occur due to a decrease in the flow rate when the stroke of the reversible operating means (4) diminishes, or the stroke of the reversible operating means (4) biases on the expanding or contracting side to facilitate the creation of local stagnation in the fluid space sectioned by the reversible operating means (4). Namely, there can be notified the biasing abnormality of the reversible operating means (4), which could not be automatically informed in the prior arts.
- this facilitates the operator's judgment as to abnormalities in the medical pump, which conducts to reductions both in monitoring mistakes of the operator and in monitoring labors thereof.
- the passage detecting means (34) detects the excessive value.
- the informing means (53) gives information on the abnormality in response to the foregoing detection.
- the information indicating this abnormality is automatically notified, whereby the operator is able to know this abnormality without monitoring the reversible operating means (4) all the time. It is therefore possible to remarkably reduce both operator's labors for monitoring and a probability of causing judgment errors and mistakes in monitoring.
- the imaging means (9) since the imaging means (9) is in non-contact with the reversible operating (4) with no element added, the operating characteristic thereof do not change at all, and the durability does not decline. Based on the imaging means and the image processing techniques of nowadays, the image of the reversible operating means (4) can accurately be picked out, and the configurational parameter thereof can also be detected with accuracy. Therefore, the flow rate informed by the informing means (53) becomes precise.
- the informing means (53) when an abnormal deformation and an abnormal deflection appear before the reversible operating means (4) is ruptured, informs the abnormalities.
- the notification about the abnormalities is given before the reversible operating means (4) is broken.
- the operator visually inspect the medical pump with confirmation in response to the abnormality information. If abnormal, the operator can take a measure of replacing the pump; otherwise a driving pressure of the pump driving module may be adjusted, and a fault detection or replacement of the pump driving module may be effected. The operator does not have to monitor the operation of the medical pump all the time, thereby decreasing both working burdens and a possibility of causing the misjudgment and monitoring mistake.
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Abstract
Description
Tg=N×[Tc-(Tup+Tdown)]
Tb=N×(Tup+Tdown)
TcD=Tc-2Tsmall
Fm=N×F
FmD=(60/TcD)×F
N×Tc=60,
and
Tb+Tg=60
Hence,
FmD=(N×Tc/TcD)
Nd=60/TcD
VmI=Vmi×30
VmO=Vmi×30
Claims (2)
Applications Claiming Priority (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1-82044 | 1989-03-31 | ||
| JP1082047A JPH02261465A (en) | 1989-03-31 | 1989-03-31 | Monitor apparatus of medical pump |
| JP1082045A JPH02261463A (en) | 1989-03-31 | 1989-03-31 | Monitor apparatus of medical pump |
| JP1-82047 | 1989-03-31 | ||
| JP1-82046 | 1989-03-31 | ||
| JP1082043A JPH02261461A (en) | 1989-03-31 | 1989-03-31 | Monitor apparatus of medical pump |
| JP1-82045 | 1989-03-31 | ||
| JP1082044A JPH02261462A (en) | 1989-03-31 | 1989-03-31 | Monitor apparatus of medical pump |
| JP1082046A JPH02261464A (en) | 1989-03-31 | 1989-03-31 | Monitor apparatus of medical pump |
| JP1-82043 | 1989-07-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US5108360A true US5108360A (en) | 1992-04-28 |
Family
ID=27524950
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/500,150 Expired - Fee Related US5108360A (en) | 1989-03-31 | 1990-03-28 | Monitoring system for medical pump |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US5108360A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4301524A1 (en) * | 1993-01-21 | 1994-07-28 | Jostra Medizintechnik | Medical unit or device for operating theaters, in particular heart-lung machine |
| US5965089A (en) * | 1996-10-04 | 1999-10-12 | United States Surgical Corporation | Circulatory support system |
| US6652447B2 (en) * | 1997-10-02 | 2003-11-25 | Micromed Technology, Inc. | Method of controlling an implantable pump system |
| US20050131271A1 (en) * | 2002-01-07 | 2005-06-16 | Micromed Technology Inc. | Method and system for physiologic control of an implantable blood pump |
| US20060241335A1 (en) * | 2002-06-26 | 2006-10-26 | Benkowski Robert J | Method and system for physiologic control of a blood pump |
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| US4687424A (en) * | 1983-05-03 | 1987-08-18 | Forschungsgesellschaft Fuer Biomedizinische Technik E.V. | Redundant piston pump for the operation of single or multiple chambered pneumatic blood pumps |
| US4775887A (en) * | 1986-02-26 | 1988-10-04 | Aisin Seiki Kabushiki Kaisha | Observation apparatus for artificial organs |
| US4865581A (en) * | 1987-05-29 | 1989-09-12 | Retroperfusion Systems, Inc. | Retroperfusion control apparatus, system and method |
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| US3465746A (en) * | 1966-03-02 | 1969-09-09 | Avco Corp | Monitor for heart pump apparatus |
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| US4597381A (en) * | 1983-11-14 | 1986-07-01 | Aisin Seiki Kabushiki Kaisha | Apparatus for monitoring an artificial internal organ |
| US4775887A (en) * | 1986-02-26 | 1988-10-04 | Aisin Seiki Kabushiki Kaisha | Observation apparatus for artificial organs |
| US4865581A (en) * | 1987-05-29 | 1989-09-12 | Retroperfusion Systems, Inc. | Retroperfusion control apparatus, system and method |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4301524A1 (en) * | 1993-01-21 | 1994-07-28 | Jostra Medizintechnik | Medical unit or device for operating theaters, in particular heart-lung machine |
| US5965089A (en) * | 1996-10-04 | 1999-10-12 | United States Surgical Corporation | Circulatory support system |
| US20040191116A1 (en) * | 1996-10-04 | 2004-09-30 | Robert Jarvik | Circulatory support system |
| US7264606B2 (en) | 1996-10-04 | 2007-09-04 | United States Surgical Corporation | Circulatory support system |
| US6652447B2 (en) * | 1997-10-02 | 2003-11-25 | Micromed Technology, Inc. | Method of controlling an implantable pump system |
| US20050131271A1 (en) * | 2002-01-07 | 2005-06-16 | Micromed Technology Inc. | Method and system for physiologic control of an implantable blood pump |
| US8323173B2 (en) * | 2002-01-07 | 2012-12-04 | Micromed Technology, Inc. | Method and system for physiologic control of an implantable blood pump |
| US20060241335A1 (en) * | 2002-06-26 | 2006-10-26 | Benkowski Robert J | Method and system for physiologic control of a blood pump |
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